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10E8.4/iMab Bispecific Antibody and VRC07-523LS Monoclonal Antibody in HIV-infected Adults

Phase 1
Active, not recruiting
Conditions
HIV-1-infection
Interventions
Drug: ART
Drug: 10E8.4/iMab
Registration Number
NCT05890963
Lead Sponsor
David Ho
Brief Summary

This is an open-label phase 1b clinical trial enrolling people living with HIV (PLWH) who are antiretroviral therapy (ART)-naïve or have not been on ART for \> 24 weeks. This study will enroll PLWH to assess the safety, tolerability, and antiviral effect of bispecific and long-acting bNAbs, alone and in combination. The study will be conducted as a single center study at National Institute for Medical Research-Mbeya Medical Research Center (NIMR-MMRC) in Mbeya, Tanzania.

20 PLWH will be sequentially enrolled into one of 5 arms, each arm comprised of 4 participants. Sequential enrollment will occur in the following order:

* Arm 1 will receive standard daily oral ART.

* Arm 2 will receive a single dose of 10E8.4/iMab 600mg intravenous injection (IV).

* Arm 3 will receive a single dose of 10E8.4/iMab 600mg intramuscular injection (IM).

* Arm 4 will receive a single dose of 10E8.4/iMab 1800mg IV.

* Arm 5 will receive a single dose of combination therapy with both 10E8.4/iMab 1800mg IV and VRC07-523LS 1200mg IV.

Detailed Description

Although global initiatives have made great strides in controlling the human immunodeficiency virus (HIV) pandemic, HIV and acquired immune deficiency syndrome (AIDS) continue to impact the lives and livelihoods of a significant portion of the population. In 2019, 38 million individuals were living with HIV and 690,000 died of AIDS-related causes. Despite extensive global efforts for disease control over the last 20 years, 1.7 million individuals contract HIV annually. Antiretroviral therapy (ART) reduces morbidity and mortality associated with HIV by suppressing viral replication but does not eradicate infection. There are barriers to universal ART use that include toxicities, costs, drug resistance, and the need for lifelong adherence. To overcome these barriers, HIV broadly neutralizing antibodies (bNAbs) represent a novel approach to HIV prevention and treatment.

The primary endpoint of change in viral load will be assessed at day 14. Participants will then transition to Step 2, during which all participants will take standard daily oral ART and have viral load monitored through Step 2 week 48.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
20
Inclusion Criteria
  1. Able to read and write in Kiswahili and/or English

  2. Able and willing to provide written informed consent

  3. Passes Test of Understanding (TOU)

  4. Aged 18-50 years, inclusive

  5. Antiretroviral Therapy (ART)-naïve or no ART for > 24 weeks at the time of screening

  6. HIV RNA 1,000-100,000 copies/mL

  7. CD4 ≥ 500 cells/mm3

  8. Laboratory criteria at screening within protocol-specified limits for blood, chemistry and urinalysis

  9. Willing and able to participate in study visits and procedures for up to 50 weeks

  10. Willing and able to begin ART as directed during the study

  11. Willing and able to use barrier protection during sex with partners without HIV or partners with unknown HIV status throughout Step 1 and until viral suppression <200 copies/mL is confirmed in Step 2

  12. Willing and able to adhere to the following contraception requirements:

    1. Participants who are able to become pregnant must agree to use at least one method of highly effective contraception if participating in sexual activity that could lead to pregnancy. This must begin at least 14 days prior to study enrollment.
    2. Participants who engage in sexual activity that could lead to their partner becoming pregnant and who are of reproductive potential must agree to use a barrier method of contraception to avoid pregnancy in a sexual partner of reproductive potential. The barrier method must be used for the duration of the study.
Exclusion Criteria
  1. Weight >100 kg
  2. Previous receipt of humanized or human monoclonal antibody whether licensed or investigational (other than for the prevention and/or treatment of SARS-CoV2/COVID-19)
  3. History of viral failure on two or more ART regimens
  4. Planned or anticipated need for enfuvirtide, maraviroc, fostemsavir, or ibalizumab for antiretroviral therapy.
  5. AIDS-defining illness, as enumerated by the WHO Stage 3 or 4, within the six months prior to enrollment
  6. Ongoing oral thrush
  7. Active injection or other recreational drug use within the previous 12 months that, in the opinion of the investigator, would impede the participant's ability to safely and consistently adhere to the study protocol
  8. History of a severe allergic reaction with generalized urticaria, angioedema or anaphylaxis in the 2 years prior to enrollment.
  9. History of chronic urticaria requiring daily treatment
  10. Known active hepatitis B virus infection or positive hepatitis B surface antigen at any time in the past
  11. Known active hepatitis C virus infection or positive hepatitis C antibody at any time in the past
  12. Untreated syphilis
  13. Estimated GFR < 50 mL/min within the past 90 days
  14. Pregnant or breast-feeding
  15. Receipt of licensed vaccine or other investigational study agent within 28 days prior to enrollment or any past participation in an investigational HIV vaccine study with receipt of active product
  16. Current or planned participation in another interventional clinical trial during the study period, including clinical trials of investigational new drugs or investigating a new application for an approved medication
  17. Chronic or recurrent use of medications that modify host immune response, such as oral steroids, parenteral steroids, or cancer chemotherapy (note: locally-acting medications-such as inhaled, topical, or intra-articular steroids-are allowed)
  18. Any other chronic or clinically significant medical condition that in the opinion of the investigator would jeopardize the safety or rights of the participant including, but not limited to: diabetes mellitus type I, chronic hepatitis, renal failure; OR clinically significant forms of: drug or alcohol abuse, mental illness, severe asthma, autoimmune disease, decompensated psychiatric disorders, hypertension, heart disease, or cancer
  19. Any medications that, in the opinion of the investigator, would preclude intramuscular injections
  20. Study site employee

Study & Design

Study Type
INTERVENTIONAL
Study Design
SEQUENTIAL
Arm && Interventions
GroupInterventionDescription
Arm 5: Combination 10E8.4/iMab and VRC07-523LS therapyVRC07-523LSParticipants will receive a single dose of combination therapy with both 10E8.4/iMab 1800mg IV. and VRC07-523LS 1200mg IV.
Arm 1: Oral ARTARTParticipants will receive standard daily oral ART.
Arm 2: 10E8.4/iMab 600mg IV.10E8.4/iMabParticipants will receive a single dose of 10E8.4/iMab 600mg IV.
Arm 3: 10E8.4/iMab 600mg IM.10E8.4/iMabParticipants will receive a single dose of 10E8.4/iMab 600mg IM.
Arm 4:10E8.4/iMab 1800mg IV.10E8.4/iMabParticipants will receive a single dose of 10E8.4/iMab 1800mg IV.
Arm 5: Combination 10E8.4/iMab and VRC07-523LS therapy10E8.4/iMabParticipants will receive a single dose of combination therapy with both 10E8.4/iMab 1800mg IV. and VRC07-523LS 1200mg IV.
Primary Outcome Measures
NameTimeMethod
Number of Grade 3 or higher antibody-related reactogenicity and adverse eventsUp to Week 48 in Step 2

Includes potentially life-threatening, or fatal events.

Change in plasma HIV RNA from day 0 to day 14Day 0 and Day 14 in Step 1

Viral RNA copies/mL will be measured.

Proportion of participants with HIV RNA < 50 copies/mL at day 14Up to Day 14 in Step 1

Percentage of participants will be calculated.

Secondary Outcome Measures
NameTimeMethod
Proportions of participants with HIV RNA <50 copies/mLUp to Week 48 in Step 2

Percentage of participants will be calculated.

Proportions of participants with HIV RNA < 200 copies/mLUp to Week 48 in Step 2

Percentage of participants will be calculated.

Proportions of participants with HIV RNA <1000 copies/mLUp to Week 48 in Step 2

Percentage of participants will be calculated.

Peripheral HIV RNAUp to Week 48 in Step 2

Serum level of viral RNA (copies/mL) will be measured.

Plasma level of 10E8.4/iMabUp to Week 48 in Step 2

Serum level of 10E8.4/iMab (ug/mL) will be measured.

Plasma level of VRC07-523LSUp to Week 48 in Step 2

Serum level of VRC07-523LS (ug/mL) will be measured.

CD4 receptor occupancyUp to Week 48 in Step 2

The percentage of CD4 cells that bind to 10E8.4/iMab will be measured.

HIV reservoir sizeUp to Week 48 in Step 2

Will measure HIV DNA in copies/million cells.

Neutralization sensitivity of 10E8.4/iMabUp to Week 48 in Step 2

Half-maximal inhibitory concentration (IC50) will be measured.

Neutralization sensitivity of VRC07-523LSUp to Week 48 in Step 2

Half-maximal inhibitory concentration (IC50) will be measured.

Presence of anti-bNAb antibodiesUp to Week 48 in Step 2

The anti-drug antibody titer in serum will be measured.

Trial Locations

Locations (1)

National Institute for Medical Research-Mbeya Medical Resarch Center

🇹🇿

Mbeya, Tanzania

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